RESPONSIBILITIES To plan and coordinate your day-to-day work in collaboration with Senior Clinical Research Facilitator. To be responsible for robust and accurate data systems of research studies. Input to governance strategies. Support and assist in the development of action plans as required. To provide data and … of studies. To provide advice and training to clinical and non-clinical Trust staff relating to clinical governance protocols, governance follow up requirements and data quality and collection. Liaise with the appropriate research teams in assisting with Local Information Packs, as required. Participate, liaise, and arrange multidisciplinary meetings across … Research Associates and the Medical and Nursing Teams, as required. Contribute to R&I strategy in growing our research portfolio. Ability to proficiently enter data onto the departmental or research management databases Delegate and refer to other research team members when risks and needs are beyond own competence and more »
as an IT Trainer or mentor Ability to rapidly familiarise self with new or bespoke applications Awareness of Information Governance policies and obligations, including DataProtectionAct and an understanding of patient data confidentiality Desirable Exposure to ITIL Practices Experience of working with clinical teams Previous … positively and maintain credibility Experience of delivering a set of agreed objectives or deliverables within the constraints of agreed policies and procedures Appreciation of dataprotection, patient confidentiality and IT security issues and knowledge of Health & Safety principles Special Circumstances Essential Able to travel between all Trust sites … and weekends if required Able to provide on-call services Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service more »
of individuals and families referred for ophthalmic research participation assisting with the coordination and delivery of planned health care as part of observational/data collection and interventional clinical trials. Supporting ERGO in contributing to the effective quality of care for patients, taking part in observational and interventional clinical … diabetic eye clinics. According to GCP guidelines - training is given to allow the Research Assistant to undertake the informed consent procedure for observational/data collection studies Maintain confidentiality of information about patients, staff and other health service business in accordance with the DataProtectionAct of 1998. To respect and maintain confidentiality of all data relating to the unit and patients, in line with GDPR May 2018 Main duties of the job Working to Good Clinical Practice Guidelines for research at all times Following the protocol of the "OKKO" study in terms of more »
The PCN has practice-based Pharmacists, Social Prescribing Link Workers, and Learning Disability Patient & Care Home Patient Coordinators. Job description Job responsibilities Clinical Care: Act as a qualified care practitioner, demonstrating advanced clinical competence and a knowledge base beyond those associated with conventional nursing roles. Triage patients on our … the Disclosure Service is available from www.disclosure.gov.uk Demonstrate professional and ethical behaviours at all times when liaising with internal and external colleagues. Under the DataProtectionAct 1998, the post holder must maintain the confidentiality of information about patients and staff. The work is of a confidential … qualified Paramedic/ANP Have completed NQP pathway (Paramedic only) Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service more »
